Polylactic acid shrink films and methods of casting same

ABSTRACT

A heat-shrinkable polylactic acid (PLA) film and a method of its manufacture are provided. In an exemplary embodiment, the PLA films exhibit heat-induced shrinkage in the transverse direction with little to no concomitant shrinkage in the machine direction. The films may comprise any grade of PLA polymer, optionally including additives, such as antiblock, slip, plasticizers, viscosity enhancers and combinations thereof. A method of cast and tenner manufacture is disclosed, which includes a temperature conditioning step.

CROSS-REFERENCE TO RELATED PATENT APPLICATIONS

This application is a continuation of U.S. patent application Ser. No.13/178,367, filed Jul. 7, 2011, which is a continuation of U.S. patentapplication Ser. No. 12/776,315, filed May 7, 2010, now U.S. Pat. No.7,998,545, which is a continuation application of U.S. patentapplication Ser. No. 11/561,771, filed Nov. 20, 2006, now U.S. Pat. No.7,713,601, which claims priority to U.S. provisional patent applicationNo. 60/738,029 filed Nov. 21, 2005, the disclosure of which have beenincorporated by reference herein in their entirety.

FIELD OF THE INVENTION

The present invention relates generally to heat-shrinkable film. Moreparticularly, the present invention relates to heat-shrinkablepolylactic acid films that exhibit temperature dependent shrinkage inone, i.e. “transverse direction,” with little to no shrinkage in theother, i.e. “machine direction.”

BACKGROUND OF THE INVENTION

Heat-shrinkable films have widely been used for various industrialapplications such as, for example, with shrink-wrap films, shrinkablelabels and cap seals, by making use of their property of heat-dependentshrinkage. The films have been applied to a variety of surfaces,including plastic and glass surfaces. Shrink films have beenmanufactured from vinyl chloride resins, polystyrene resins or polyesterresins; however, in many instances, film shrinkage is concomitant withundesirable “draw back” of the outer edges of the film (a.k.a. “smiling”or “frowning”). The undesirable draw back of the outer edges has limitedthe application of shrink films. Therefore, there is a need for shrinkfilms that have little to no draw back.

As well, interest in compostable polymers. i.e. biopolymers, has greatlyincreased, and many companies have made efforts to market, for example,packaging materials, hygiene products, sacks, and films with compostablepolymers. Polylactic acid (PLA), i.e., polylactide, or condensationpolymers which are based on lactic acid, are for many reasons a veryattractive group of biopolymers. Their principal degradation product,lactic acid, is a product common in nature, it is not toxic and is usedwidely in the food and pharmaceutical industries.

PLA films can be manufactured by either blown film or casting (e.g.,cast and tenner) techniques. While either method has advantages anddrawbacks, the cast film is generally better suited for certain end-userapplications, such as those requiring film “sleeves” rather than“wrap-around” film. Further, cast film generally has much better opticsthan a blown film and can be produced at higher line speeds. However,PLA films that are manufactured by current casting methods exhibitexcessive shrinkage in the machine direction, which substantiallycontributes to curling and limits their range of application. Thus,there is a need for PLA shrink films manufactured by casting methodsthat exhibit little to no shrinkage in the machine direction.

SUMMARY OF THE INVENTION

The foregoing needs are met, to an extent, by the present invention,wherein in one embodiment shrink film comprised of a transversedirection oriented PLA polymer blend film is provided which, uponexposure to heat, exhibits shrinkage in the transverse direction andless than about 10% shrinkage in the machine direction. In a preferredembodiment, the shrinkage in the machine direction does not exceed about5%. The shrink film may exhibit shrinkage in the transverse direction inthe range of about 10% to about 80% and exhibit a shrinkage in themachine direction in the range of about 0% to about 5% when subjected toabout 60° C. heat for about 10 seconds. In some embodiments, the shrinkfilm may exhibit shrinkage in the transverse direction of about 30% toabout 80% and exhibit shrinkage in the machine of about 0% to about 3%when subjected to about 60° C. heat for about 10 seconds. In otherembodiments, the shrink film may exhibit shrinkage in the transversedirection of about 25% and exhibit a shrinkage in the machine directionof about 0% or less (a negative value indicates growth) when subjectedto about 60° C. heat for about 10 seconds.

The inventive PLA shrink films may further comprise one or moreadditives, such as an antiblock additive, a slip additive, a viscosityenhancer or a combination thereof. The antiblock additive may be naturalsilica, synthetic silica, talc, talc filled magnesium, calciumcarbonate, and N,N′-Ethylene Bis(Stearamide) (EBS). The preferredantiblock additive in some embodiments is talc filled magnesium. Theslip additive may be oleamide, erucamide, stearamide, behenamide, oleylpalmitamide, stearyl erucamide, ethylene bis-oleamide, EBS, or acombination thereof, and preferably EBS in some embodiments. Viscosityenhancers may include, for example, stabilizers or coupling agents. Apreferred coupling agent is CESA®-extend.

The PLA polymer blends of the inventive shrink films disclosed hereinmay include two or more “grades” of PLA polymer. For example, PLApolymer may comprise about 1 to about 2 percent by weight D-lactide;about 3 to about 5 percent by weight D-lactide; or about 11 to about 13percent by weight D-lactide. In some embodiments, the shrink films maycomprise about 50 weight percent to about 90 weight percent of PLApolymer having about 11 to about 13 percent by weight D-lactide; andabout 10 weight percent to about 50 weight percent of a PLA polymerhaving about 1 to about 2 percent by weight D-lactide. In otherembodiments, the shrink films may comprise about 60 weight percent toabout 80 weight percent of PLA polymer having about 11 to about 13percent by weight D-lactide; and about 20 weight percent to about 40weight percent of a PLA polymer having about 1 to about 2 percent byweight D-lactide. In yet other embodiments, the shrink films maycomprise about 65 weight percent to about 75 weight percent of PLApolymer having about 11 to about 13 percent by weight D-lactide; andabout 25 weight percent to about 35 weight percent of a PLA polymerhaving about 1 to about 2 percent by weight D-lactide.

Further, the present invention provides films comprising about 50 weightpercent to about 90 weight percent of PLA polymer having about 11 toabout 13 percent by weight D-lactide; about 10 weight percent to about50 weight percent of a PLA polymer having about 1 to about 2 percent byweight D-lactide; less than about 3 percent by weight of an antiblockadditive; less than about 1 percent of a slip additive; and less thanabout 0.5 percent of a viscosity enhancer. The inventive films may alsocomprise about 50 weight percent to about 90 weight percent of PLApolymer having about 11 to about 13 percent by weight D-lactide; about10 weight percent to about 50 weight percent of a PLA polymer havingabout 1 to about 2 percent by weight D-lactide; less than about 2percent by weight of an antiblock additive; less than about 0.5 percentof a slip additive; and less than about 0.25 percent of a viscosityenhancer. Preferably, in some embodiments, the inventive shrink filmscomprise about 50 weight percent to about 90 weight percent of PLApolymer having about 11 to about 13 percent by weight D-lactide; about10 weight percent to about 50 weight percent of a PLA polymer havingabout 1 to about 2 percent by weight D-lactide; less than about 1percent by weight of an antiblock additive; less than about 0.25 percentof a slip additive; and less than about 0.1 percent of a viscosityenhancer.

In accordance with another embodiment of the present invention, apackaged good is provided comprising a consumable item and a heattreated sleeve over at least a portion of the consumable item, whichheat treated sleeve is obtained by exposing to heat a PLA shrink filmcomprised of a PLA polymer blend which exhibits shrinkage in thetransverse direction and less than about 10%, preferably less than about5%, shrinkage in the machine direction upon exposure to heat. Thepackaged good may be a consumable item, including batteries, cans,bottles, disposable lighters, pens and decorative items. The sleeve mayform a perforated or non-perforated neck band around the consumable itemand may be clear, matte, translucent, or opaque. The packaged good withthe heat treated sleeve may include a packaging label and the label maybe printed onto the film.

In yet another embodiment of the present invention, a method of making ashrink film is provided comprising: (a) providing dry pellets of PLA,(b) melting the pellets to form a molten mass, (c) extruding theresulting molten mass, (d) casting the extrusion between at least threecasting rollers to form a film, (e) adjusting the temperature of thefilm, and (f) stretching the film in the transverse direction. Themethod may optionally include drying the pellets, for example, in adehumidifying hopper, prior to melting the pellets to form a moltenmass.

The melting step may be carried out at a temperature may range fromabout 165° C. to about 230° C., preferably from about 170° C. to about200° C., and more preferably at about 175° C. The extruding may takeplace though a T style die, and the temperature conditioning of the filmmay take place in a machine direction orienting (“MDO”) machine, whichmay further be equipped with one or more idler rollers. The stretchingmay be carried out in a tenner machine, preferably at a temperatureranging about 70° C. to about 90° C., more preferably at about 80° C. Insome embodiments of the disclosed invention, the method may furtherinclude annealing the film. The annealing may be carried out at atemperature ranging from about 50° C. to about 90° C., preferably atabout 70° C. with a overall shrink back of 1%-5%

In further yet another embodiment of the present invention, castingmachine with three or more rollers is provided. The three or morerollers may be motorized and/or temperature controlled.

There has thus been outlined, rather broadly, certain embodiments of theinvention in order that the detailed description thereof herein may bebetter understood, and in order that the present contribution to the artmay be better appreciated. There are, of course, additional embodimentsof the invention that will be described below and which will form thesubject matter of the claims appended hereto.

In this respect, before explaining at least one embodiment of theinvention in detail, it is to be understood that the invention is notlimited in its application to the details of construction and to thearrangements of the components set forth in the following description orillustrated in the drawings. The invention is capable of embodiments inaddition to those described and of being practiced and carried out invarious ways. Also, it is to be understood that the phraseology andterminology employed herein, as well as the abstract, are for thepurpose of description and should not be regarded as limiting.

As such, those skilled in the art will appreciate that the conceptionupon which this disclosure is based may readily be utilized as a basisfor the designing of other structures, methods and systems for carryingout the several purposes of the present invention. It is important,therefore, that the claims be regarded as including such equivalentconstructions insofar as they do not depart from the spirit and scope ofthe present invention.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a schematic diagram of the movement of polymer film from a diethrough casting and MDO machines and then to a tenner machine inaccordance with one embodiment of the present invention. The pathwaythrough the casting machine and tenner machine is illustrated witharrows. A general outline of the respective machines is provided bydashed lines. Circles represent rollers.

FIG. 2 is a graph depicting the percent shrinkage of a cast PLA film(“TDO”) of the present invention at a given temperature for ten secondscompared to blown PLA film (“MDO”). Both machine direction (MD) andtransverse direction (TD) shrinkage is provided.

FIG. 3 is a graph depicting the percent TD shrinkage of the inventivePLA TDO films in relation to non-PLA TDO films. PLA: Polylactic Acid;TMOPS: Transverse Mono-Oriented Polystyrene; PETG: Glycol ModifiedPolyethylene Terephthalate; PVC: Polyvinyl Chloride.

FIG. 4 is a graph depicting the percent MD shrinkage of the inventivePLA TDO films in relation to non-PLA TDO films.

DETAILED DESCRIPTION

In one embodiment of the instant invention, plastic films and a methodof their manufacture are described. The polymer films are generatedthat, when heat treated, shrink in the transverse direction and exhibitlittle to no shrinkage in the machine direction. In a preferredembodiment, the shrink films of the invention exhibits a shrinkage, uponheating, in the transverse direction of no less than about 40%,preferably no less than about 50%, and most preferably no less thanabout 60%. Similarly, in a preferred embodiment, the shrink films of theinvention exhibits a shrinkage, upon heating, in the machine directionof no greater than about 10%, preferably no greater than about 5%, evenmore preferably no greater than about 3%, and most preferably about 0%or less (a negative value indicates growth). The shrinkage in eitherdirection preferably occurs substantially simultaneously.

The machine direction will be defined herein as the “longitudinal” or“length” direction. The “transverse direction, also termed “crossdirection” or “cross web direction,” will be defined herein as thedirection perpendicular to the machine direction. Embodiments of filmsdescribed herein exhibit reduced edge-curling characteristics and can beproduced in clear, matte, translucent colors and opaque colors. Films ofthe present invention may be suitable for hack side and/or front sideprinting.

Films of the present invention may comprise various polymers and polymergrades of polylactic acid (“PLA”) known in the art. Preferably, in someembodiments, polymers are selected that, when used alone or in a blend,enable “memory” to be stored from an orienting process described herein.Many of the determinants for polymer selection are known to one ofordinary skill in the art and/or will be apparent from the teachingsherein. For example, where high temperature processing is desired,polymers with higher softening points may be selected, such as, forexample, relatively high molecular weight polymers.

Shrink films of the instant invention comprise PLA, and may optionallyinclude additives known in the art, e.g., antiblock additives, slipadditives, plasticizers and “viscosity enhancers.” These additives aregenerally employed to enhance the processing, performance and look ofthe final product as will be discussed below. In each of theaforementioned classes, various grades of the respective polymers areunderstood to be included. Each of these classes of polymers andadditives will now be discussed, in turn, as relevant to the instantinvention.

PLA

Since both lactic acid and lactide can achieve the same repeating unit,the general term polylactic acid as used herein refers to polymershaving the repeating unit of formula I without any limitation as to howthe polymer was made (e.g., from lactides, lactic acid, or oligomers),and without reference to the degree of polymerization.

The polylactide used in the invention may be made from L-, D- orD,L-lactide, or blends thereof, by any polymerization process. A highmolecular weight polymer can be produced by ring-opening polymerizationfrom lactic acid dimer, lactide. Lactic acid is optically active, andthus its dimer appears in four different forms: L,L-lactide;D,D-lactide; L,D-lactide (“mesolactide”); and a racemic mixture of L,L-and D,D-lactides. By polymerizing these dimers either as pure compoundsor at different blend proportions, polymers are obtained which havedifferent stereochemical structures affecting their resilience andcrystallinity and, consequently, also their mechanical and thermalproperties. The obtained polymers are usually hard and optically clear.

Copolymers or polymer blends may also be used in PLA films of thepresent invention. The weight-average molecular weight (Mw) of polymerssuitable to the invention is approximately 10,000-400,000, preferably40,000-250,000.

Polylactide is in equilibrium with its monomer, lactide. This chemicalproperty can lead to rapid hydrolysis and cause problems of adhesion inthe processing of the polymer. Furthermore, the presence of the monomerlowers thermal stability during melt processing. Therefore, residuallactide is typically and preferably removed from the polymer. Preferablemonomer content is preferably below about 2%, and more preferably belowabout 1%.

Heat, during film processing steps, may also contribute to polymerdegradation. In addition to the removal of lactide monomer, another wayto retard premature hydrolysis of the polymer is to reduce the watercontent of the polymer to below 500 ppm, and more preferably, to below200 ppm. Methods to further reduce and/or maintain low water content aredescribed herein below.

PLA is available from multiple suppliers and the polymers and/or polymerblends of the instant invention are not limited to any one grade orsupplier thereof. However, NatureWorks® polymers, as supplied byCargill, Inc. are preferred in some embodiments of the instant invention(e.g., grades 4060D, 4042D, 4032D). While each of grades 4060D, 4042Dand 4032D has a molecular weight average 200,000 to about 400,000, theyare prepared with differing percentages of D-lactide. Grade 4042D isprepared with about 3 to about 5 weight percent D-lactide. Grade Grade4060D comprises about 11 to about 13 percent D-lactide; grade 4032Dpolymer comprises about 1 to about 2 percent D-lactide. These polymersare supplied with a lactide concentration of lower than about 1 percent,a mesolactide level of about 10 percent to about 20 percent, and amoisture level lower than about 500 ppm.

While the instant invention can be suited with any PLA polymer of anygrade and composition, the concentration of D-lactide, in particular,can affect the physical properties of the resulting PLA polymer. By wayof example, increasing the percent of D-lactide in a polymer or apolymer blend reduces the capacity of the resulting polymer tocrystallize, which, in turn, increases undesirable degradation of thepolymer at higher temperatures. Said another way, lowering the weightpercent of D-lactide in a polymer composition increases the temperatureresistance of the polymer and hence the viscosity of the resulting meltat a given temperature as well.

Polymers and/or polymer blends with higher levels of D-lactide can yieldfilms that begin to shrink at lower temperatures when exposed to heat;these films also tend to exhibit more “gentle” shrink curves, i.e., lessshrinkage per rise in temperature. Conversely, films comprising polymerswith relatively low D-lactide concentration generally require exposureto higher temperatures to shrink. It should also be noted that,typically, PLA polymers with lower concentrations of D-lactide are moreexpensive than otherwise equivalent polymers having greater D-lactide.Therefore, there can be an economic incentive to maximize the use of PLAwith higher levels of D-lactide; however, this incentive should and canbe balanced with the desired physical properties of the films.

Antiblock Additives

Antiblock (also called “antitack”) additives serve to improve processingand application of polymer films. Specifically, this class of additivesis used to reduce the adhesion between films. Antiblock agents—typicallyfinely divided, solid minerals, but also waxes act by producing a slightroughening of the surface. Antiblock agents are mainly used in filmextrusion and include natural silica, synthetic silica, talc, calciumcarbonate, and N,N′-Ethylene Bis(Stearamide) (EBS).

Antiblock additives are typically “loaded” with a carrier compound.While it is by no means a requirement, it is preferable that the carrierpolymer be similar to or equivalent to one or all of the polymers in themaster PLA blend. In the instant invention, for example, it is preferredthat the carrier polymer be a PLA polymer. As the “active ingredient” inan antiblock comprises only a small fraction of the final composition,adding a carrier compound provides ease and consistency in measurements.One of ordinary skill in the art would recognize to take theconcentration of filler into account when calculating the finalconcentration of antiblock in the final product. For example, if acomposition comprising 10 percent antiblock consists of 10 percent“active ingredient,” the final concentration of the “active ingredient”is 1.0 percent of the total. The values hereinbelow, including those inTables 1 and 2, are provided as a percentage of the “active ingredient”in the final formulation.

In the instant invention, the final concentration of antiblock is lessthan about 3 percent by weight, preferably less than about 2 percent byweight, and more preferably less than about 1 percent by weight. In oneembodiment of the present invention, antiblock 2100D from Cargill ispreferred. 2100D comprises 10% talc filled magnesium silicate in grade4032D PLA carrier and has a mean particle size of less than about 1micron.

In selecting an appropriate antiblock agent, the particle size thereofis one factor to consider. Indeed, the particle size of an antiblockagent can directly contribute to the overall smoothness of the resultingfilm. That is, all other factors being equal, a smaller antiblockparticle size will result in a smoother film. Another factor to consideris the concentration of the antiblock. The concentration of antiblock ispreferably minimized particularly, as in some cases, because antiblockadditives can introduce haze to the film. Hence, particularly inapplications where haze is undesirable (e.g., envelope windows, etc.),the concentration of antiblock may be minimized.

Slip Additives/Processing Aids

Processing aids refer to a class of agents that generally aid in thedownstream manufacturing (i.e., post-extrusion operations) of thevarious film products. Slip additives, for example, are modifiers thatact as an internal lubricant to reduce the coefficient of friction (COF)between two overlapping films, for example, in films rolled afterproduction. Indeed, lower COFs are especially desirable for filmapplications. These additives migrate to the surface of the plasticduring and immediately after processing. That is, a non-visible coating“blooms” to the surface to provide a microscopic “layer” of air betweentwo adjacent sheets of film. In this way, enhanced lubricity and slipcharacteristics are provided.

Accordingly, slip additives may be considered similar to antiblockadditives in that they both serve to lower the COF between twooverlapping films. Films of the instant invention may comprise one, bothor neither class of additives. Typical slip agents are, for example,oleamide, erucamide, stearamide, behenamide, oleyl palmitamide, stearylerucamide, ethylene bis-oleamide, EBS, including most grades of theirrespective refinement. In some embodiments, EBS is a preferred slipagent, and EBS with 4032D carrier is more preferred. These and otherslip additives and processing aids are commercially available under thefollowing trade names: Adogen 42, Armid 18, Crodamide VRX, E, ER, andBR, Danimer 9205, Freeflow Z100 and Z200, Incromold, Incroslip,Kemamides, Kemamide P-181, MoldWiz Int-33CRS, Paraloid EXL, Uniwax 1750and Viton. EBS is sold under the trade names Advawax, Lubrol EA andMicotomic 280.

As with antiblock agents, the “active ingredient” of slip additives isgenerally supplied with a carrier. Films of the instant inventioncomprise less than about 1 percent by weight of a slip additive(referring to the “active ingredient” only), and more preferably lessthan about 0.5 percent by weight. It should be noted that excessiveamounts of slip additive may produce films that are excessively smooth,which can compromise the ability of substances (e.g., ink, stickers,etc.) to adhere to the surface. Thus, to enhance, for example, theprinting properties of shrink films of the instant invention, the amountof slip additive may require adjustment accordingly.

Plasticizers

While practice of the present invention does not require the use ofimpact modifiers (a.k.a. “plasticizers”), their use may be beneficial inprocessing. For example, some plasticizers can reduce brittleness. Manyplasticizers are known in the art and the present invention is notlimited in their use herein. Non-limiting examples include: commonlyavailable commercial plasticizers, for example, mono- and polycarboxylicacid esters, polymeric polyesters, polyalkyl ethers, glycerol and glycolesters (e.g., glycerol triacetate and glycerol tripropionate), lowmolecular weight aliphatic and aromatic polyesters, and blends ofthereof. Also various polymeric plasticizers such as citrate esters,adipate esters, epoxidized soy oils, acetylated coconut oil, linseedoil, and mixtures thereof are suitable. As well, it is commonlyappreciated that the addition of lactic acid, lactides (including, D-and L-lactide, meso and racemic D,L-lactide), oligomers of lactic acid,oligomers of lactide, and mixtures thereof, in a PLA blend may act asplasticizers of the polymer.

Viscosity Enhancers

Although numerous methods are known and available to increase theviscosity of polymers during processing of cast and tenner films, theterm “viscosity enhancer” is defined herein to encompass any chemicalagent that increases or maintains the viscosity of a polymer at a giventemperature. Viscosity enhancers may be introduced into the polymerblend at any time until the polymer enters the die (discussed below),however, viscosity enhancers are preferably introduced prior toextrusion, and more preferably, during blending of the polymer pellets.

Viscosity enhancers can improve the finished properties of films bypreventing and/or reversing the degradation encountered duringprocessing of polymer films. Some viscosity enhancers are “stabilizers.”That is, they are used in virgin plastic to either (1) protect againstdegradation in processing and/or (2) reverse the degradation caused byrecycling, and return the plastic to nearly its original performanceproperties. Another class of viscosity enhancers, “coupling agents,” forexample, improves the processability of extruded polymer by “coupling”individual polymer strands thereby increasing the melt strength of theplastic.

Viscosity enhancers are generally known and available to one of ordinaryskill in the art and have their broadest application with polyesters,polyamides (nylon) and polycarbonates. Though the chemical identity ofviscosity enhancers is generally proprietary, the products are availablefrom vendors such as Johnson Polymer LLC (USA) and ClariantInternational Ltd. (Switzerland). Viscosity enhancers suitable in theinstant invention are not limited to those exemplified and/or those withsimilar mechanisms. In fact, any chemical agent that increases ormaintains the viscosity of a polymer at a given temperature may suffice.

In a preferred embodiment of the invention, shrink films are generatedcomprising a coupling agent for enhancing viscosity. One such couplingagent, CESA®-extend, is available from Clariant. These viscosityenhancers contain a proprietary copolymer of styrene, methylmethacrylate and glycidyl methacrylate. Without being limited by orbound to theory, CESA®-extend viscosity enhancers are thought to repairthe damage (e.g., polymer breakdown) that heat and moisture can cause toPLA resins by coupling individual PLA polymers. In this way, theviscosity enhancer may “extend” polymer chains in the presence of somedegradation and thereby attenuate overall loss of molecular weight andviscosity of the polymer melt.

Optimum reactivity of CESA®-extend can be achieved with a preferable uselevel of less than about 0.15 percent by weight, and preferably lessthan about 0.75 percent by weight of the active ingredient. Again, the“active ingredient” of viscosity enhancers is generally supplied with acarrier. CESA®-extend viscosity enhancers may undergo a processresidence time of about 2 to about 20 minutes, depending on startingmoisture and/or inherent starting viscosity of the polymer. As well,process residence times are preferably minimized to attenuate polymerdegradation from the heat required in the process. A detailed discussionof processing conditions is provided below. In any event, one ofordinary skill in the art would appreciate that it may be necessary toadjust the concentration of any polymer enhancer based, at least, onsome of the factors listed above.

In some embodiments, polymers for films may be selected from one or moreof five groups (i.e., PLA, antiblock and slip additives, plasticizers,viscosity enhancers) and combined to create blended polymer films.Tables 1 and 2 below provides non-limiting examples of formulations thatmay be suitable in the preparation of films of the present invention.For clarity in description, a skilled artisan should appreciate from theteachings herein that the percent of additives calculated is only the“active ingredient.” In other words, while it should be appreciated thatthe additives are generally supplied in as a combination of “activeingredient” and carrier, the percent of carrier, if any, has not beenlisted.

TABLE 1 Polymer Formulations Composition (percentage by weight) Visc.No. 4060D 4042D 4032D Antiblock Slip Enhancer 1 69.58%    0%   30% 0.15%0.18% 0.09% 2 97.50%    0%    0% 1.50% 0.50% 0.50% 3    0%    0% 99.58%0.15% 0.18% 0.09% 4    0%    0% 97.50% 1.50% 0.50% 0.50% 5    0% 98.58%   0% 0.15% 0.18% 0.09% 6    0%   98%    0% 1.50% 0.50% 0.50% 7 98.58%   0%    0% 0.15% 0.18% 0.09% 8 59.58%   10%   30% 0.15% 0.18% 0.09% 949.58%   20%   30% 0.15% 0.18% 0.09% 10 39.58%   30%   30% 0.15% 0.18%0.09% 11 48.61%   30%   20% 1.12% 0.18% 0.09% 12   48%   30%   20% 1.00%0.50% 0.50% 13   30%   20%   48% 1.00% 0.50% 0.50% 14   30%   30% 39.58%0.15% 0.18% 0.09% 15   30%    0% 68.85% 0.15% 0.50% 0.50% 16 68.85%   0%   30% 0.15% 0.50% 0.50% 17    0% 68.85%   30% 0.15% 0.50% 0.50% 18  30% 68.85%    0% 0.15% 0.50% 0.50% 19 29.58%   30%   40% 0.15% 0.18%0.09% 20   70%    0%   29% 0.50% 0.25% 0.25% 21   29%    0%   70% 0.50%0.25% 0.25% 22   99%    0%    0% 0.50% 0.25% 0.25% 23    0%   99%    0%0.50% 0.25% 0.25% 24    0%    0%   99% 0.50% 0.25% 0.25% 25   100%    0%   0%   0%   0%   0% 26    0%   100%    0%   0%   0%   0% 27    0%    0%  100%   0%   0%   0% 28    0%    0%    0%  100%   0%   0% 29 99.63%   0%    0% 0.10% 0.18% 0.09% 30    0% 99.63%    0% 0.10% 0.18% 0.09% 31   0%    0% 99.63% 0.10% 0.18% 0.09% 32 99.68%    0%    0% 0.05% 0.18%0.09% 33    0% 99.68%    0% 0.05% 0.18% 0.09% 34    0%    0% 99.68%0.05% 0.18% 0.09% 35   30%   30% 39.68% 0.05% 0.18% 0.09% 36 39.68%  30%   30% 0.05% 0.18% 0.09% 37    0% 39.68%   30% 0.05% 0.18% 0.09% 38  70%    0%  29.3%  0.1%  0.6%   0%

TABLE 2 Polymer Formulations Composition (percentage by weight) No.4060D 4042D 4032D Antiblock Slip Plasticizer 39 70% 0% 24.3% 0.10% 0.60%5% 40 70% 1% 24.3% 0.10% 0.60% 4% 41 65% 5% 26.3% 0.10% 0.60% 3% 42 68%2% 28.3% 0.10% 0.60% 1% 43 70% 5% 24.3% 0.10% 0.60% 0% 44 70% 0% 29.3%0.10% 0.60% 0% 45 70% 0% 24.5% 0.10% 0.40% 5% 46 70% 0% 24.7% 0.10%0.20% 5% 47 70% 0% 24.3% 0.05% 0.65% 5% 48 70% 0% 24.3% 0.15% 0.55% 5%49 70% 0% 24.3% 0.25% 0.45% 5%

The blends in Tables above may be chosen or prepared to create the“feel” or flexibility of the film to match an end-use application. Whereall other processing parameters are equal, the ratio of PLA polymers maybe adjusted in accordance with the teachings of the instant invention toprovide shrink films with desirable physical properties. For example,reducing the concentration of D-lactide (i.e., increasing weight percent4032D) yields polymers with a higher softening point and films thatrequire greater temperature to shrink, which moves the shrink curve tothe right.

While the formulations listed in the tables above have been categorizedbased on the presence of a viscosity enhancer (Table 1) or a plasticizer(Table 2), formulations of the present invention may include both aviscosity enhancer and a plasticizer. Furthermore, all formulations(i.e., PLA polymer blends) may include one or more “color correction”dyes. Such dyes, known and available to those of ordinary skill in theart, are typically added to tint films (e.g., from a yellow to blueindex) so to make them better suited for printing thereon. Theconcentration of color correction dyes generally ranges from about0.002%-0.009%, preferably about 0.006%, by weight.

In a preferred embodiment, films are produced with a blend of about 94weight percent PLA polymer and less than about 6 percent additives byweight and in which the PLA polymer component is about 70 percent 4060DPLA and 24 percent 4032D by weight. In another preferred embodiment,films are produced with a polymer blend according to formula no. 39.

Processing

After the polymer composition of the film is selected, the polymer isthen processed to generate a film with desirable shrink properties.Generally, the polymers are procured in pellets or grains. In caseswhere multiple polymers are to be included, the polymers pellets arefirst dry blended. That is, the pellets are mixed together. In apreferred embodiment of the invention, the pellets are then processedinto film by cast and tenner technology.

Cast and tenner processing involves the extrusion of polymers meltedthrough a slot or flat die to form a thin, molten sheet or film. Thisfilm is first “polished” by the surface of a chill roll (typicallytemperature-regulated and chrome-plated). The film is then rolledthrough a machine direction orienting (“MDO”) machine for temperatureconditioning and stretched through a tenner frame. Finally, the filmedges are slit prior to winding.

Thus, the cast and tenner method can be characterized in four essentialsteps: extrusion, casting, temperature conditioning and stretching. Apreliminary step of drying the polymer pellets is preferable, but notrequired. As well, a terminal step of annealing may be preferable, butnot required according to the instant teachings. An assembly for eachprocessing step is generally depicted in FIG. 1 and will now bedescribed in detail.

Drying

PLA polymers are generally supplied in sealed bags from the manufacturerand in relatively dry condition. Typically, the moisture content ofthese as-supplied PLA polymers is less than about 500 ppm and preferablyless than about 200 ppm. Where the moisture level is deemed desirable,no further drying may be necessary or required. However, PLA readilyabsorbs moisture from the atmosphere and therefore, the blended polymerpellets are optionally and preferably first dried by heating in a dryerto remove surface moisture. Without being bound by or limited to theory,it is believed that the removal of moisture content may help control therelative viscosity loss due to hydrolysis. As mentioned above, highertemperatures and the presence of even a small amount of moisture canhydrolyze PLA in the ensuing melt phase.

PLA is generally produced by a reversible condensation reaction, whichproduces water; when undried PLA is heated, hydrolysis can occur and keymechanical properties of the PLA may be compromised. For example, theviscosity of the polymer, when melted, is inversely proportional to thepercentage of free monomer therein. Therefore, in an attempt to minimizebatch-to-batch variation in viscosity, preferably, significant moistureis removed from the polymer pellets. In some embodiments, a moisturecontent of less than about 200 ppm is preferable, and less than about 50ppm, more preferable (measured by the Karl Fisher method).

A dehumidifying hopper with hot air at a relatively low dew point may beused; however, a variety of air dryers are known in the art and many ofthem may be suitable for drying. The present invention need not belimited to air dryers only, but may include other types of dryers,including baking ovens. A dehumidifying hopper may be desirable in someembodiments in that dehumidified air passes through a bed of PLA toextract moisture from the resin. A desiccant material, such as silica,absorbs moisture from the circulating air. Dual desiccant bed systemsare common, so that one bed is on-stream while a stand-by bed is beingregenerated. Either a time-cycle or a predetermined decrease in air dewpoint is used to shift airflow from one bed to the other. Suchmethodology is thought to be effective in removing some moisture thatmay reside below the surface of the polymer pellets in addition to thesurface moisture.

Preferable dryers of the instant invention for drying PLA may have oneor more of the following characteristics:

-   1. Desiccant beds capable of achieving a dew point of about −40° C.    in the supply air-   2. A means, e.g., an after-cooling unit, to eliminate or reduce the    likelihood of a temperature spike in the supply air-   3. Superior temperature control in the PLA drying range

The temperature and duration of drying may be dependent on the totalamount and condition of the polymer(s) (i.e., the amount of startingsurface moisture), and may need to be adjusted on a batch-by-hatchbasis. Preferably, the polymers experience little to no melting in thisstep. By way of example, typical drying conditions require thattemperatures range from about 40° C. to about 110° C., and preferablyfrom about 55° C. to about 90° C. for variable periods of time. By wayof specific example, the residence time for drying polymer with air (dewpoint, −40° C.) at a flow rate of greater than about 0.5 ft³/min.requires about 4 hours at about 40° C. and about 2 hours at about 90° C.Higher drying temperatures may lead to softening and blocking ofpolymer, while lower drying temperatures can result in extended dryingtimes and/or incomplete drying.

Dew point is an absolute measure of air moisture and is independent ofair temperature. Dew point may be used to control dryer performance.Airflow is another component to drying, as it heats the resin andabsorbs its moisture. Sufficient airflow can maintain the resin at theproper temperature for its entire residence time. In embodiments wereadditional colorants, additives, or otherwise ingredients are used, itmay be preferable to minimize moisture-related degradation by furtherdrying same.

Extrusion

Extrusion is whereby the pellets are melted into a low viscosity moltenmass, thus combining the heretofore individual polymer beads or grainsinto one molten mass. The viscosity of the melt will depend on thetemperature. Temperatures can range from about the temperature at whichthe polymers will remain melted to about the temperature wheredegradation of the polymers begins to occur. By way of example,extrusion melt temperatures may be maintained between about 165° C. toabout 230° C. for certain PLA polymer blends, but may ultimately dependon the different polymers that have been blended and their respectivemelting points. In some embodiments, about 175° C., is preferred.

The molten plastic is then extruded thought a T style die with a flatslot opening. The opening should be adjusted to accommodate thethickness of the finished film. In other words, a greater opening shouldbe used where thicker films are desired and vice versa. Generally, theopening will range between about 0.01 inches to about 0.10 inches andpreferably between about 0.05 inches to about 0.07 inches. The draw-downdistance (i.e., the distance from the die to the casting rollers) canalso affect the thickness of the resultant film. Generally, the longerthe distance, the thinner the film, and vice versa. Without beinglimited to or bound by theory, it is believed that the greater draw-downdistances introduce undesirable machine direction orientation into theresultant film. Thus, while draw-down distances may range from 0.75inches to about 1.5 inches, shorter distances are preferred. A draw downdistance of about 0.750 inches is generally appropriate.

Casting

The relatively hot (e.g., about 175 to about 190° C.) plastic from theextruder is then “cast” between at least two rollers. Without beinglimited by or bound by theory, the temperature of the casting rollersshould be adjusted to achieve rapid cooling over the exterior of theextrudate so as to form a “skin,” which causes the extrudate to adhereto the rollers. At the same time, the temperature of the rollers shouldbe maintained high enough so that the “core” of the extrudate remainspliable so to allow curving around the rollers without breakage orcracking.

Typical casting machines in the art are equipped with one or tworollers, wherein the plastic moves from the die, between a single largeroller or two rollers and then on to the machine direction orientationmachine. The present inventors have discovered, however, that while thetypical casing machines are suitable in preparing the inventive filmsdisclosed herein, the novel use of a third roller in the casting machineis preferable in the production of the films, particularly whereimproved surface quality of the films is desired. In fact, it isbelieved that the use of three or more rollers in the production of PLAfilm, more particularly thin gauge PEA film (e.g., less than about 0.002in. film) has not been performed.

The use of a third or more roller(s) is believed to be one reason forsignificantly improved production speed. Whereas film is typically castat about 130 feet/minute, the process described herein provides a linespeed of about 250 feet/minute. Without being limited to or bound bytheory, it is believed that the additional roller(s) aids in theequilibration of the hotter core temperature with the cooler skintemperature. Accordingly, this third roller(s) is preferably maintainedat a higher temperature than the first two rollers.

By way of example, all of the casting rollers may be set at a relativelycold temperatures (e.g., about 20 to about 45° C., preferably about 30°C. to about 40° C., for the first two rollers, and about 40 to about 65°C., preferably about 55 to about 60° C., for the third roller). Thetemperature of the rollers are may be maintained with liquids, such aswater, oil. Water is a preferable coolant for the casting rollersbecause of its greater heat capacity than most conventional liquids.Typically, water can remove three times more heat (BTU) than oils forthis purpose.

One of ordinary skill in the art should appreciate from the teachingspresented herein, that the absolute temperature of the rollers willdepend on several factors, including the initial temperature andthickness of the extruded plastic. Thus, the roller temperaturesprovided herein should not be construed as limiting to all theembodiments of the instant invention, but rather exemplary of a rangefor certain embodiments. Rather, the temperature of the rollers can andshould be adjusted based on the thickness of the die opening, stretchratio and the like. In one embodiment, for example, the first roller isset at about 40° C., the second at about 32° C. and the third at about57° C.

In fact, more significant than the absolute temperature, any castingroller is the temperature of the extruded film as it exits the castingmachine. The temperature of the film as it exits the casting machine ispreferably between about 55° C. and about 75° C., and more preferablyabout 60° C.

In addition to adjusting the temperature of the plastic as it arrivesfrom the die, the casting rollers can also be used to adjust thethickness of the plastic. This adjustment is made by presetting the gapbetween the roller to the desired thickness. For example, the gapbetween the first two rollers is preferably 2-10 times, more preferably5-7 times, the final desired thickness of the film. Similarly, the gapbetween the second and third rollers is preferably 3-9 times, morepreferably 4-6 times, the final desired thickness of the film.

Temperature Conditioning

The next step in preparation of films of the present invention is atemperature conditioning step. “Temperature conditioning” refers to theprocess of equilibrating the temperature of the plastic film such thattemperature difference between the core and skin, if any at all, isminimized. While an MDO machine may be used in this process, orientation(i.e., stretching) in the machine direction (“MD”) is preferablyminimized because MD stretching leads to undesirable MD shrinking.

A variety of measures may be taken to limit or avoid MD stretching whenusing an MDO machine. For example, the speed to the MDO rollers may beadjusted to minimize “pulling” the film from one roller to the next. Forexample, the rollers may be maintained at similar speeds. (A film is atrisk of being pulled when a subsequent roller turns faster than the oneprior.) Alternatively, the distance between and location of the MDOrollers can contribute to MD stretching. For example, lateral movementof film typically is pulled less than horizontal movement.

The present inventors have found the novel use of “idler” rollers tobypass some MDO rollers to be beneficial to reducing MD stretching. Idlerollers are not motor driven and therefore “idle” unless film is passedover them. Idle rollers may, but need not, be temperature controlled.The number and location of idle rollers is not limiting and may beadjusted to suit specific processing parameters. In one embodiment ofthe present invention, two idle rollers are installed to bypass twocentral rollers in an MDO machine (FIG. 1, A and B).

As with the casting rollers, more significant than the absolutetemperature of any MDO roller is the temperature of the film as it exitsthe MDO machine. Indeed, the roller temperature may have to be adjustedin accordance with film thickness, desired stretch, etc. Preferably, thetemperature of the film is equilibrated to between about 60° C. to about90° C., and more preferably, about 70° C. In one embodiment of theinvention, an MDO machine with 6 motorized, and two idle rollers areused as shown in FIG. 1: roller 4 is at about 72° C., roller 5 is atabout 85° C., idle rollers 6 and 7 are not temperature controlled,roller 8 is at about 85° C., and roller 9 is at about 60° C.

Tenner

Once the extrudate has been temperature conditioned, it enters thetenner machine. This machine is equipped with tenner clips that cliponto the edge of the plastic film, which is generally about 20 incheswide. The tenner machine is fitted with an “A-frame” that stretches theplastic film to about 4 times its entering width (e.g., from 20 inchesto 80 inches).

The tenner machine further consists of three temperature controlledzones along the A-frame. The preheating zone is provided to uniformlyraise the temperature of the polymer and ensure that the film coretemperature has equilibrated with the skin temperature. The stretchingzone maintains proper stretching temperature. It should be appreciatedfrom the teachings herein that the stretch temperature will need to beadjusted based on the particular PLA blend, practices and experienceavailable to one of ordinary skill in the art. In one embodiment,however, this temperature is shared with the preheating zone, which isbetween about 70° C. and about 90° C., more preferably about 80° C. Thefinal zone is the annealing zone.

Annealing

Annealing, also called crystallization or relaxation, is typically thefinal step in the preparation of films of the instant invention.According to the teachings herein, an annealing step is optional. Whendesired, annealing is generally accomplished post-stretching and isperformed at temperatures between about 49° C. to about 90° C.,preferably about 70° C. During annealing, the film “relaxes” to a smallextent. Relaxation rates of about 0.5% to about 5% are typical, andabout 3% or less is preferred. Lastly, the edges of the stretched filmare trimmed and wound onto rollers by conventional means.

Film properties using the aforementioned protocol can be manipulated asdesired with nominal trial and error by one of ordinary skill in theart. Such variations are expected and are incorporated into the scope ofthe invention. Films of the instant invention can generally havecharacteristics that fall into the following ranges:

Film Shrinkage at about 60° C. for about 10 seconds:

Transverse direction: about 10% to about 70%, with an average of about25%.

Machine direction: about −2% to about 1%, with an average of about 0%.

In one embodiment of the instant invention, percent shrinkage as afunction of temperature was studied with, for example, 200 gauge (0.002in.) film subjected to 10 second exposures to heat (FIG. 2). The filmstested herein were prepared from a blend of about 70% grade 4060D PLA,about 26% grade 4032D PLA, about 1% grade 2100D antiblock of which 10%is “active ingredient,” and about 3% slip EBS, of which 20% is activeingredient. (The term “about” has been used herein and throughout thisspecification to account for the customary variations in measurements ofmass, temperature and percent shrinkage common and expected by one ofordinary skill practicing this art.)

Using the process described above, the polymer blend, without additionaldrying, was extruded at about 190° C., and was subsequently extrudedthrough a T style die with an opening of about 0.070 inches. The filmwas then cast between three rollers at about 40° C., 32° C., and 57° C.in sequence yielding a film temperature of about 65° C. The film wasthen temperature conditioned in an MDO machine equipped with sixmotorized rollers and two idler rollers as shown in FIG. 1. This stepyielded a film temperature of about 70° C. Finally, the film was 4×stretched in a tenner machine, annealed at about 70° C., trimmed andwound.

The film were placed in a hot water bath at the temperature shown forthe indicated times, and the shrinkage in the machine direction (MD) andthe transverse direction (TD) as a percentage of the original dimensionswas plotted. While the shrink films studied in this example weresubjected to heated water, exposure to heat in any form (e.g., heatedair from a hot air dryer) may induce shrinkage of the inventive films.As is evident from the results, the films described exhibit shrinkage inthe TD and little to no shrinkage in the MD. At about 60° C., forexample, the inventive film shrinks more than 25% in the TD and lessthan 1% in the MD.

The shrink properties of the inventive films were also compared with PLAblown film (FIG. 2) and cast/termer films comprising polymers other thanPLA (FIGS. 3 and 4). FIG. 2 shows that the instant films (“TDO”) exhibitgreater shrinkage than blown “MDO” films in the TD at a giventemperature. FIG. 3 demonstrates that the TD shrink curve of the instantPLA films, while comparable in magnitude, occurs at a lower temperaturethan non-PLA TDO films. For example, TDO PLA can shrink over 60% in theTD at about 70° C. whereas TDO PETG must be heated to about 80° C. toshrink the same amount. Effective shrinkage at lower temperatures isparticularly desirable in applications where heat may be detrimental tothe packaged product, such as, for example, with dairy products. Thus,the inventive PLA TDO films outperform PETG TDO where pre-labeledbottles (e.g., milk and/or dairy packaging) are preferably kept at thecoolest operable temperature. Finally, FIG. 4 shows that (1) the instantfilms have shrinkage in the MD concomitant with shrinkage in the MD and(2) this shrinkage can occur at relatively low temperatures. PETG TDO,for example, shrinks in the MD before shrinkage in the TD, which resultsin undesirable drawing back at the edges.

This growth in the cross direction can prevent the label from curlingback on the edges during the shrinking process. Accordingly, in oneembodiment, films of the present invention may have application insleeve (i.e., tube) labeling of various shaped cylinders and cones suchas, for example, batteries, cans, bottles, disposable lighters, pens,floral wraps and other decorative items. However, the scope ofapplications should not be limited to the aforementioned consumerproducts or uses.

Films of the present invention have innumerable other applications. Forexample, these films can also be used in printed/unprinted applicationfor holding together twin packs, attachments, neck bands, and perforatedneck hands for decoration or tamper evident use, to name a few options.

The many features and advantages of the invention are apparent from thedetailed specification, and thus, it is intended by the appended claimsto cover all such features and advantages of the invention, which fallwithin the spirit and scope of the invention. Further, since numerousmodifications and variations will readily occur to those skilled in theart, it is not desired to limit the invention to the exact constructionand operation illustrated and described, and accordingly, all suitablemodifications and equivalents may be resorted to, fall within the scopeof the invention.

What is claimed is:
 1. A packaged good comprising a shrink filmcomprising polylactic acid (PLA) polymer blend which, upon exposure to60° C. heat for 10 seconds, exhibits shrinkage in the transversedirection of 10% to 50% of the original dimension and shrinkage in themachine direction that does not exceed 10% of the original dimension,wherein the PLA polymer blend comprises: (a) 65 weight percent to 75weight percent of PLA polymer having 11 to 13 percent by weightD-lactide; and (b) 10 weight percent to 20 weight percent of a PLApolymer having 1 to 2 percent by weight D-lactide.
 2. The packaged goodof claim 1, in which the film shrinkage in the machine direction doesnot exceed 5% of the original dimension.
 3. The packaged good of claim1, comprising a battery, can, bottle, disposable lighter and/or pen. 4.The packaged good of claim 1, wherein the film further comprises 5weight percent to 25 weight percent of one or more additives.
 5. Thepackaged good of claim 4, in which the one or more additives is aantiblock additive, a slip additive, a plasticizer, a viscosity enhanceror a combination thereof.
 6. The packaged good of claim 5, in which theantiblock additive is selected from the group consisting of naturalsilica, synthetic silica, talc, talc filled magnesium, calciumcarbonate, and N,N′-Ethylene Bis(Stearamide) (EBS).
 7. The packaged goodof claim 5, in which the slip additive is selected from the groupconsisting of oleamide, erucamide, stearamides, behenamide, oleylpalmitamide, stearyl erucamide, ethylene his-oleamide, EBS, or acombination thereof.
 8. The packaged good of claim 7, in which theviscosity enhancer is a stabilizer or a coupling agent.